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Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia

Preeclampsia (PE) is characterized by great endothelial dysfunction, decreased nitric oxide (NO) bioavailability, and higher levels of arginase activity. In the present study, we investigated the potential modulatory effects of trans-resveratrol (RSV) on arginase and endothelial dysfunction biomarke...

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Autores principales: Bueno-Pereira, Thaina Omia, Bertozzi-Matheus, Mariana, Zampieri, Gabriela Morelli, Abbade, Joelcio Francisco, Cavalli, Ricardo C., Nunes, Priscila Rezeck, Sandrim, Valeria Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686533/
https://www.ncbi.nlm.nih.gov/pubmed/36358483
http://dx.doi.org/10.3390/antiox11112111
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author Bueno-Pereira, Thaina Omia
Bertozzi-Matheus, Mariana
Zampieri, Gabriela Morelli
Abbade, Joelcio Francisco
Cavalli, Ricardo C.
Nunes, Priscila Rezeck
Sandrim, Valeria Cristina
author_facet Bueno-Pereira, Thaina Omia
Bertozzi-Matheus, Mariana
Zampieri, Gabriela Morelli
Abbade, Joelcio Francisco
Cavalli, Ricardo C.
Nunes, Priscila Rezeck
Sandrim, Valeria Cristina
author_sort Bueno-Pereira, Thaina Omia
collection PubMed
description Preeclampsia (PE) is characterized by great endothelial dysfunction, decreased nitric oxide (NO) bioavailability, and higher levels of arginase activity. In the present study, we investigated the potential modulatory effects of trans-resveratrol (RSV) on arginase and endothelial dysfunction biomarkers in endothelial cells exposed to plasma from patients with PE and healthy pregnant (HP) women, and umbilical arteries from patients with PE. Human umbilical vein endothelial cells (HUVECs) were incubated with pooled plasma from 10 HP or 10 PE pregnant women and RSV; umbilical arteries from patients with PE were incubated with RSV; intracellular NO and total reactive oxygen species (ROS) levels were assessed using a probe that interacted with these radicals; total arginase activity was evaluated measuring the urea produced; total antioxidant capacity was measured using the ferric reduction ability power (FRAP) assay; and endothelial dysfunction biomarkers were assessed using qPCR in endothelial cells and umbilical arteries. RSV increased NO levels and decreased total arginase activity in endothelial cells incubated with plasma from patients with PE. In addition, RSV increased total antioxidant capacity and downregulated endothelial dysfunction biomarkers, such as intercellular adhesion molecule-1 (ICAM-1), von Willebrand factor (vWF), and Caspase-3, (CASP-3), in endothelial cells and umbilical arteries from PE patients. RSV treatment positively modulated the (L)-arginine–NO pathway, decreased arginase activity, and increased antioxidant capacity, in addition to downregulating endothelial dysfunction biomarkers.
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spelling pubmed-96865332022-11-25 Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia Bueno-Pereira, Thaina Omia Bertozzi-Matheus, Mariana Zampieri, Gabriela Morelli Abbade, Joelcio Francisco Cavalli, Ricardo C. Nunes, Priscila Rezeck Sandrim, Valeria Cristina Antioxidants (Basel) Article Preeclampsia (PE) is characterized by great endothelial dysfunction, decreased nitric oxide (NO) bioavailability, and higher levels of arginase activity. In the present study, we investigated the potential modulatory effects of trans-resveratrol (RSV) on arginase and endothelial dysfunction biomarkers in endothelial cells exposed to plasma from patients with PE and healthy pregnant (HP) women, and umbilical arteries from patients with PE. Human umbilical vein endothelial cells (HUVECs) were incubated with pooled plasma from 10 HP or 10 PE pregnant women and RSV; umbilical arteries from patients with PE were incubated with RSV; intracellular NO and total reactive oxygen species (ROS) levels were assessed using a probe that interacted with these radicals; total arginase activity was evaluated measuring the urea produced; total antioxidant capacity was measured using the ferric reduction ability power (FRAP) assay; and endothelial dysfunction biomarkers were assessed using qPCR in endothelial cells and umbilical arteries. RSV increased NO levels and decreased total arginase activity in endothelial cells incubated with plasma from patients with PE. In addition, RSV increased total antioxidant capacity and downregulated endothelial dysfunction biomarkers, such as intercellular adhesion molecule-1 (ICAM-1), von Willebrand factor (vWF), and Caspase-3, (CASP-3), in endothelial cells and umbilical arteries from PE patients. RSV treatment positively modulated the (L)-arginine–NO pathway, decreased arginase activity, and increased antioxidant capacity, in addition to downregulating endothelial dysfunction biomarkers. MDPI 2022-10-26 /pmc/articles/PMC9686533/ /pubmed/36358483 http://dx.doi.org/10.3390/antiox11112111 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bueno-Pereira, Thaina Omia
Bertozzi-Matheus, Mariana
Zampieri, Gabriela Morelli
Abbade, Joelcio Francisco
Cavalli, Ricardo C.
Nunes, Priscila Rezeck
Sandrim, Valeria Cristina
Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title_full Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title_fullStr Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title_full_unstemmed Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title_short Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia
title_sort markers of endothelial dysfunction are attenuated by resveratrol in preeclampsia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686533/
https://www.ncbi.nlm.nih.gov/pubmed/36358483
http://dx.doi.org/10.3390/antiox11112111
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